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					<label>Versions et origines des bases de données</label>
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						Base
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						Origine
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						Version
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						Dernière mise à jour
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						DGV
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						<a href="http://projects.tcag.ca">Database of Genomic Variants</a>
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						variation.hg19.v10.nov.2010.txt + indel.hg19.v10.nov.2010.txt
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						9/06/2011
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						ISCA
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						<a href="https://www.iscaconsortium.org/index.php/array-analysis-toolbox"></a>
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						GRCh37/hg19 : Pathogenic Likely Pathogenic Uncertain Likely Benign Benign 2011-09-19
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						22/11/2011
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						Micro remaniements
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						<a href="https://decipher.sanger.ac.uk">Decipher syndromes</a>
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						Decipher V5.1 GRch37
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						8/06/2011
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						GENE NCBI
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						<a href="">Map viewer</a>
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						11/01/2012
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						Sites fragiles
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						<a href="http://www.sciencedirect.com/science/article/pii/S0304383505008268">The molecular basis of common and rare fragile sites. Michal Schwartz, Eitan Zlotorynski and Batsheva Kerem.</a>
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						Table 1 de l'article
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						Passage en NCBI37 effectué via <a href="http://www.ncbi.nlm.nih.gov/genome/tools/remap/">NCBI Genome Remapping Service</a> le 22/06/2011
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						Redon
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						<a href="http://www.sanger.ac.uk/humgen/cnv/redon2006/cnv_data/">Global CNV Assessment (Redon 2006): Data</a>
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						Redon_CNVs
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						Passage en NCBI37 effectu� via <a href="http://www.ncbi.nlm.nih.gov/genome/tools/remap/">NCBI Genome Remapping Service</a> le 8/06/2011
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						CNPc
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						Calcul� sur la base des CNV de VisioPuce de Montpellier au 20/06/2011
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						Calcul� sur la base des CNV de VisioPuce de Montpellier au 20/06/2011
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						CNP Lyon
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						Fichier donné par Damien Sanlaville mi 2011
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						CNP Nantes, Lyon, Rouen et Rennes
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						Fichier donné par Cédric Le Caignec Bioinfo_CNV_herite 081111.xls
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